15270
Biuret
98% (Contains ≤10%(w/w) Triuret)
Sinónimos:
Allophanic acid amide, Carbamoylurea
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Fórmula lineal:
NH2CONHCONH2
Número CAS:
Peso molecular:
103.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-559-0
Beilstein/REAXYS Number:
1703510
MDL number:
Assay:
98% (Contains ≤10%(w/w) Triuret)
Form:
powder or crystals
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Permítanos ayudarleInChI key
OHJMTUPIZMNBFR-UHFFFAOYSA-N
InChI
1S/C2H5N3O2/c3-1(6)5-2(4)7/h(H5,3,4,5,6,7)
SMILES string
NC(=O)NC(N)=O
assay
98% (Contains ≤10%(w/w) Triuret)
form
powder or crystals
impurities
≤1% water
mp
185-190 °C (dec.) (lit.)
functional group
amine
Quality Level
Categorías relacionadas
Application
Biuret (Carbamoylurea) was used as a source of dietary nitrogen in purified diets for steers.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Evaluation of urea, biuret, urea phosphate and uric acid as NPN sources for cattle.
R R Oltjen et al.
The Journal of nutrition, 94(2), 193-202 (1968-02-01)
Shuping Jin et al.
Journal of agricultural and food chemistry, 59(1), 322-327 (2010-12-16)
In this investigation, a novel water-insoluble slow-release fertilizer, biuret polyphosphoramide (BPAM), was formulated and synthesized from urea, phosphoric acid (H(3)PO(4)), and ferric oxide (Fe(2)O(3)). The structure of BPAM was characterized by Fourier transform infrared (FTIR) spectroscopy. Subsequently, a coated slow-release
S J Woltman et al.
Journal of pharmaceutical and biomedical analysis, 14(1-2), 155-164 (1995-12-01)
An electrochemical detection method was applied to the determination of the synthetic peptide TP9201 (Telios Pharmaceuticals). The method utilizes reversed-phase HPLC, followed by post-column formation of Cu(II)-peptide complexes to render peptides electrochemically active via the Cu(III/II) couple. TP9201 is cyclic
C L Kuckel et al.
Biochimica et biophysica acta, 1162(1-2), 143-148 (1993-03-05)
Uremia has been implicated in cataractogenesis due to protein carbamylation by cyanate derived from urea. The present study was designed to directly identify the effects of carbamylation on actin polymerization and the possible contribution to cataract formation. The susceptibility of
S M Rutherfurd et al.
Amino acids, 32(2), 235-242 (2006-07-27)
The stability of felinine, an amino acid present in feline urine, was investigated. Synthetic felinine was unstable in the urine of a selection of mammals. Felinine was found to stable in feline urine in which urea had been degraded. Synthetic
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